chr16-53631425-G-A

Position:

• chr16-53631425-G-A

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_015272.5(RPGRIP1L):​c.3294+5014C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.481 in 152,082 control chromosomes in the GnomAD database, including 21,581 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.48 (21581 hom., cov: 32)
• Consequence: RPGRIP1L NM_015272.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.29

Genes affected

RPGRIP1L (HGNC:29168): (RPGRIP1 like) The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). [provided by RefSeq, Jun 2016]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.819 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
RPGRIP1L	NM_015272.5	c.3294+5014C>T		intron_variant		ENST00000647211.2	NP_056087.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
RPGRIP1L	ENST00000647211.2	c.3294+5014C>T		intron_variant			NM_015272.5	ENSP00000493946.1

Frequencies

GnomAD3 genomes AF: 0.481 AC: 73082 AN: 151964 Hom.: 21519 Cov.: 32

Gnomad AFR AF: 0.826

Gnomad AMI AF: 0.311

Gnomad AMR AF: 0.468

Gnomad ASJ AF: 0.379

Gnomad EAS AF: 0.613

Gnomad SAS AF: 0.417

Gnomad FIN AF: 0.200

Gnomad MID AF: 0.519

Gnomad NFE AF: 0.319

Gnomad OTH AF: 0.476

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.481 AC: 73200 AN: 152082 Hom.: 21581 Cov.: 32 AF XY: 0.475 AC XY: 35309 AN XY: 74316

Gnomad4 AFR AF: 0.826

Gnomad4 AMR AF: 0.468

Gnomad4 ASJ AF: 0.379

Gnomad4 EAS AF: 0.613

Gnomad4 SAS AF: 0.417

Gnomad4 FIN AF: 0.200

Gnomad4 NFE AF: 0.319

Gnomad4 OTH AF: 0.482

Alfa AF: 0.361 Hom.: 5297

Bravo AF: 0.517

Asia WGS AF: 0.532 AC: 1853 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	5.9
DANN	Benign	0.53

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs1077352; hg19: chr16-53665337;